The purpose of this study is to assess the safety and efficacy of Bimatoprost/Timolol Fixed Combination in the treatment of glaucoma or ocular...
Date First Received: May 30, 2006
Last Updated: May 30, 2006
Verified by: Allergan, April 2006
Clinical Trial Phase: Phase 3 | Start Date: August 2001
Overall Status: Completed
Estimated Enrollment: 480
Brief Summary
Condition Keyword(s):
Intervention(s):
The purpose of this study is to assess the safety and efficacy of Bimatoprost/Timolol Fixed Combination in the treatment of glaucoma or ocular hypertension
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study
Intervention(s) in this Clinical Trial
- Drug: bimatoprost/timolol fixed combination
Outcome Measures for this Clinical Trial
Primary Measures
- IOP
Criteria for Participation in this Clinical Trial
Inclusion Criteria:
- Clinical diagnosis of ocular hypertension or chronic glaucoma in both eyes
- Patient needs IOP-lowering drug in both eyes
Exclusion Criteria:
- Uncontrolled medical condition
- Contraindication to beta-adrenoceptor antagonist therapy
Gender Eligibility for this Clinical Trial: Both
Minimum Age for this Clinical Trial: 18 Years
Maximum Age for this Clinical Trial: N/A
Are Healthy Volunteers Accepted for this Clinical Trial?: No
Clinical Trial Sponsor Information
Lead Sponsor: Allergan
Additional Information
Information obtained from ClinicalTrials.gov on November 19, 2008
Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00332072
Study ID Number: 192024-021T
ClinicalTrials.gov Identifier: NCT00332072
Health Authority: United States: Food and Drug Administration
Clinical Trials Authorship and Review
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